GB765642A - Improvements in or relating to silicone-alkyd resins - Google Patents

Improvements in or relating to silicone-alkyd resins

Info

Publication number
GB765642A
GB765642A GB8613/55A GB861355A GB765642A GB 765642 A GB765642 A GB 765642A GB 8613/55 A GB8613/55 A GB 8613/55A GB 861355 A GB861355 A GB 861355A GB 765642 A GB765642 A GB 765642A
Authority
GB
United Kingdom
Prior art keywords
per cent
alcohol
acid
dicarboxylic
trimethylolethane
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB8613/55A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Midland Silicones Ltd
Original Assignee
Midland Silicones Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Midland Silicones Ltd filed Critical Midland Silicones Ltd
Publication of GB765642A publication Critical patent/GB765642A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/42Block-or graft-polymers containing polysiloxane sequences
    • C08G77/445Block-or graft-polymers containing polysiloxane sequences containing polyester sequences

Abstract

A silicone-alkyd resin consists essentially of the reaction product of (1) 5 to 60 per cent (by weight) of an organosilicon compound of the general formula RnSiXmO4-n-m/2, wherein each R is a monovalent hydrocarbon or halogenated hydrocarbon radical, each X is a halogen atom, alkoxy or hydroxy radical, n has an average value of 1 to 2 and m has an average value of 0.05 to 3; (2) 10 to 35 per cent of alcohol composed of 20 to 100 per cent by weight, calculated on the total alcohol content, of trimethylolethane, 0 to 50 per cent of a dihydric alcohol and 0 to 30 per cent of another trihydric alcohol; and (3) 20 to 60 per cent of a dicarboxylic acid, anhydride or lower alkyl ester (i.e. containing less than 9 carbon atoms) thereof. The preferred method of making the resins comprises the single stage reaction of (1) 5 to 60 per cent of the organosilicon compound, (2) 10 to 35 per cent of alcohol composed of 50 to 100 per cent of trimethylolethane and 0 to 50 per cent of a dihydric alcohol, and (3) 20 to 60 per cent of a lower alkyl ester of a dicarboxylic acid, at 100 DEG to 250 DEG C. until the desired viscosity is obtained. The reaction may be effected in the presence of a catalyst such as magnesium acetate or perfluoroglutaric acid. Reactants specified are: (1) dimethyldichloro-, dibutyldi-isopropoxy-, phenylmethyldichloro, divinyldibutoxy-, tolyltriethoxy, cyclohexyl-trimethoxy-, phenylmethyldibromo-, (trifluoromethylphenyl) methyldichloro-, chlorophenyltriethoxy-, bromoxenyltrichloro-, stearylmethyldiethoxy and allylstearyloxydimethoxy-silanes, mixtures and hydrolysates thereof, diphenyl-, phenylmethyl-, dimethyl-, chlorophenylmethyl- and octadecylmethyl-silanediols; (2) ethylene glycol, neopentylglycol and glycerine; (3) malonic, adipic, maleic, dimethylmaleic, cyclohexyldicarboxylic, phthalic, terephthalic, isophthalic, naphthalic, stilbene dicarboxylic, diphenic, tolane dicarboxylic and dibenzyl dicarboxylic acids, their anhydrides and alkyl esters containing less than 9 carbon atoms. In a modification up to 50 per cent of (1) may be replaced by a drying oil and/or drying oil acid, e.g. linseed, sardine, soyabean, dehydrated castor, tung, oiticica, perilla, chinawood, hemp seed, poppy seed, safflower, sunflower or walnut oil or acid derived therefrom. The resins may be dissolved in solvents such as acetonyl alcohol, naphtha, isophorone or cresylic acid or solvent mixtures such as diacetone alcohol and butyrolactone; petroleum hydrocarbons, isophorone and methylamylacetate; acetonyl acetone and diacetone alcohol; and C6H5.OCH2.CH2.OOC.CH3 and diacetone alcohol, and used for coating metal surfaces, particularly fine wire. Examples are given. Specification 663,599 is referred to.
GB8613/55A 1954-05-28 1955-03-24 Improvements in or relating to silicone-alkyd resins Expired GB765642A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US765642XA 1954-05-28 1954-05-28

Publications (1)

Publication Number Publication Date
GB765642A true GB765642A (en) 1957-01-09

Family

ID=22132814

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8613/55A Expired GB765642A (en) 1954-05-28 1955-03-24 Improvements in or relating to silicone-alkyd resins

Country Status (1)

Country Link
GB (1) GB765642A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0075326A1 (en) * 1981-09-23 1983-03-30 Dow Corning Corporation Non-precondensed silicone-alkyd resins and a method for their preparation

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0075326A1 (en) * 1981-09-23 1983-03-30 Dow Corning Corporation Non-precondensed silicone-alkyd resins and a method for their preparation

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